The readability of informed consent forms for research studies conducted in South Africadoi:10.7196/SAMJ.2021.v111i2.14752Fischer, A. E.Venter, W. D. F.Collins;, S.Carman, M.Lalla-Edward, S. T.SAMJ: South African Medical Journal
Consent forms in research are a source of current and retrospective information for the subject, a “prompt” for the person who is obtaining consent, and a documentation of the “informed” consent process and its adequacy. Occasionally, these forms may be administered by inexperienced trainees or...
Readability standards for informed-consent forms as compared with actual readability. N Engl J Med. 2003;348(8):721-726. doi:10.1056/NEJMsa021212 PubMedGoogle ScholarCrossref 2. Albala I, Doyle M, Appelbaum PS. The evolution of consent forms for research: a quarter ...
Many ethics review bodies now routinely recommend the use of written consent forms as the default method of obtaining informed consent, including for research conducted in African countries. Although it is generally possible for researchers to justify the use of alternative methods, this is not always...
Examining the ethics of human subjects research. Only a small number of studies examine the research consent process. Nevertheless, existing data strongly [End Page 283] suggest that subject recruitment ... PS Appelbaum - 《Kennedy Institute of Ethics Journal》 被引量: 46发表: 1996年 加载更多研...
Informed Consent Forms are required for all studies and medical procedures. When working with limited English proficiency (LEP) individuals, researchers must translate forms, provide interpreters, and make necessary accommodations. If this blog has helped clarify Informed Consent Form translations, please ...
Ideally, translated consent forms should be back-translated and compared with the original to ensure accuracy. For review purposes, both the local language and the English version of the ICF should be submitted. For multi-centre research studies, a common consent form will be taken as a ...
For multi-centre research studies, a common consent form will be taken as a minimum requirement to which additions may be made as dictated by local circumstances. In such cases, the common consent form should be written in either the researcher's mother tongue, or the language which the ...
BACKGROUND: Many subjects enrolled in research studies have a limited understanding of the research to which they consented. OBJECTIVE: To develop recommendations to enhance comprehensiveness and understanding of informed consent forms used in critical care clinical trials. DESIGN: Consensus process. RECOMM...
Health literacy and consent forms: librarians support research on human subjects. Journal of the Medical Library Association : JMLA, 102(1)... PG Raimondo,RL Harris,M Nance,... - 《Journal of the Medical Library Association》 被引量: 0发表: 2014年 case studies health literacy and consent ...